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Prevention Research

Abstract 2590: Curcumin inhibits prostate cancer metastasis in vivo by targeting the inflammatory cytokines CXCL1 and -2.

Peter H. Killian, Emanuel Kronski, Simonetta Astigiano, Ottavia Barbieri, Christian P. Sommerhoff, Andreas G. Nerlich, Ulrich Pfeffer and Beatrice E. Bachmeier
Peter H. Killian
1Ludwig-Maximilians-University, Munich, Germany;
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Emanuel Kronski
1Ludwig-Maximilians-University, Munich, Germany;
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Simonetta Astigiano
2National Cancer Research Institute, Genoa, Italy;
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Ottavia Barbieri
2National Cancer Research Institute, Genoa, Italy;
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Christian P. Sommerhoff
1Ludwig-Maximilians-University, Munich, Germany;
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Andreas G. Nerlich
3Academic Hospital Munich-Bogenhausen, Munich, Germany.
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Ulrich Pfeffer
2National Cancer Research Institute, Genoa, Italy;
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Beatrice E. Bachmeier
1Ludwig-Maximilians-University, Munich, Germany;
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DOI: 10.1158/1538-7445.AM2013-2590 Published April 2013
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Proceedings: AACR 104th Annual Meeting 2013; Apr 6-10, 2013; Washington, DC

Abstract

In America and Western Europe prostate cancer is the second leading cause of death in men. Emerging evidence suggests that chronic inflammation is a major risk factor for the development and metastatic progression of prostate cancer.

We previously reported that the chemopreventive polyphenol Curcumin inhibits the expression of the pro-inflammatory cytokines CXCL1 and -2 leading to diminished formation of breast cancer metastases. Here we analyse the effects of Curcumin on prostate carcinoma growth, apoptosis and metastasis. We show that Curcumin inhibits translocation of NFκB to the nucleus through the inhibition of the IκB-kinase, IKKβ, leading to stabilization of the inhibitor of NFκB, IκBα, in PC3 prostate carcinoma cells. Inhibition of NFκB activity reduces expression of CXCL1 and -2 and abolishes the autocrine/paracrine loop that links the two chemokines to NFκB. The combination of Curcumin with the synthetic IKKβ inhibitor, SC-541, shows no additive or synergistic effects indicating that the two compounds share the target. Treatment of the cells with Curcumin as wells as siRNA based knock-down of CXCL1 and -2 induce apoptosis, inhibit proliferation, and down-regulate several important metastasis-promoting factors like COX2, SPARC, and EFEMP. In an orthotopic mouse model of haematogenous metastasis, treatment with Curcumin inhibits statistically significantly formation of lung metastases.

In conclusion, chronic inflammation can induce a metastasis prone phenotype in prostate cancer cells by maintaining a positive pro-inflammatory and pro-metastatic feed-back loop between NFκB and CXCL1/-2. Curcumin disrupts this feed-back loop by the inhibition of NFκB signalling leading to reduced metastasis formation in vivo.

Citation Format: Peter H. Killian, Emanuel Kronski, Simonetta Astigiano, Ottavia Barbieri, Christian P. Sommerhoff, Andreas G. Nerlich, Ulrich Pfeffer, Beatrice E. Bachmeier. Curcumin inhibits prostate cancer metastasis in vivo by targeting the inflammatory cytokines CXCL1 and -2. [abstract]. In: Proceedings of the 104th Annual Meeting of the American Association for Cancer Research; 2013 Apr 6-10; Washington, DC. Philadelphia (PA): AACR; Cancer Res 2013;73(8 Suppl):Abstract nr 2590. doi:10.1158/1538-7445.AM2013-2590

  • ©2013 American Association for Cancer Research
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Cancer Research: 73 (8 Supplement)
April 2013
Volume 73, Issue 8 Supplement
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Abstract 2590: Curcumin inhibits prostate cancer metastasis in vivo by targeting the inflammatory cytokines CXCL1 and -2.
Peter H. Killian, Emanuel Kronski, Simonetta Astigiano, Ottavia Barbieri, Christian P. Sommerhoff, Andreas G. Nerlich, Ulrich Pfeffer and Beatrice E. Bachmeier
Cancer Res April 15 2013 (73) (8 Supplement) 2590; DOI: 10.1158/1538-7445.AM2013-2590

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Abstract 2590: Curcumin inhibits prostate cancer metastasis in vivo by targeting the inflammatory cytokines CXCL1 and -2.
Peter H. Killian, Emanuel Kronski, Simonetta Astigiano, Ottavia Barbieri, Christian P. Sommerhoff, Andreas G. Nerlich, Ulrich Pfeffer and Beatrice E. Bachmeier
Cancer Res April 15 2013 (73) (8 Supplement) 2590; DOI: 10.1158/1538-7445.AM2013-2590
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